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Hereditary sensory and autonomic neuropathy type 1
4 OMIM references -
4 associated genes
23 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant spastic paraplegia type 3
Burkitt lymphoma
Congenital bilateral absence of vas deferens
Cystic fibrosis
Follicular lymphoma
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Intravascular large B-cell lymphoma
Male infertility with normal virilization due to meiosis defect
Precursor T-cell acute lymphoblastic leukemia
Primary mediastinal large B-cell lymphoma
Apolipoprotein A-I deficiency
Tangier disease
Giant cell glioblastoma
Gliosarcoma
Young adult-onset Parkinsonism
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
4 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
ATL1 Q8WXF7606439
ATL3 Q6DD88609369
SPTLC1 O15269605712
SPTLC2 O15270605713
No signs/symptoms info available.